KR950018021A - 활성 분자를 위한 벡타로서의 인지질. 그의 제조 방법 및 화장품 또는 외피용 조성물에서의 그의 용도 - Google Patents
활성 분자를 위한 벡타로서의 인지질. 그의 제조 방법 및 화장품 또는 외피용 조성물에서의 그의 용도 Download PDFInfo
- Publication number
- KR950018021A KR950018021A KR1019940036836A KR19940036836A KR950018021A KR 950018021 A KR950018021 A KR 950018021A KR 1019940036836 A KR1019940036836 A KR 1019940036836A KR 19940036836 A KR19940036836 A KR 19940036836A KR 950018021 A KR950018021 A KR 950018021A
- Authority
- KR
- South Korea
- Prior art keywords
- acid
- active
- phospholipid
- skin
- cosmetic
- Prior art date
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- 150000003904 phospholipids Chemical class 0.000 title claims abstract 16
- 239000000203 mixture Substances 0.000 title claims abstract 12
- 239000002537 cosmetic Substances 0.000 title claims abstract 11
- 238000000034 method Methods 0.000 title claims 7
- 230000002500 effect on skin Effects 0.000 title claims 2
- 239000013598 vector Substances 0.000 title claims 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract 13
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims abstract 8
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims abstract 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract 6
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims abstract 6
- 208000002874 Acne Vulgaris Diseases 0.000 claims abstract 4
- 206010000496 acne Diseases 0.000 claims abstract 4
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 claims abstract 3
- SQUHHTBVTRBESD-UHFFFAOYSA-N Hexa-Ac-myo-Inositol Natural products CC(=O)OC1C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O SQUHHTBVTRBESD-UHFFFAOYSA-N 0.000 claims abstract 3
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 claims abstract 3
- 125000001931 aliphatic group Chemical group 0.000 claims abstract 3
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 3
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 claims abstract 3
- 229960001231 choline Drugs 0.000 claims abstract 3
- CDAISMWEOUEBRE-GPIVLXJGSA-N inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 claims abstract 3
- 229960000367 inositol Drugs 0.000 claims abstract 3
- 229920006395 saturated elastomer Polymers 0.000 claims abstract 3
- CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 claims abstract 3
- 206010013786 Dry skin Diseases 0.000 claims abstract 2
- 230000037336 dry skin Effects 0.000 claims abstract 2
- 238000004519 manufacturing process Methods 0.000 claims abstract 2
- 239000002253 acid Substances 0.000 claims 17
- 150000001875 compounds Chemical class 0.000 claims 5
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 4
- -1 farnesyl succinate Chemical compound 0.000 claims 4
- 239000000126 substance Substances 0.000 claims 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 3
- 150000007513 acids Chemical class 0.000 claims 3
- MBMBGCFOFBJSGT-KUBAVDMBSA-N all-cis-docosa-4,7,10,13,16,19-hexaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCC(O)=O MBMBGCFOFBJSGT-KUBAVDMBSA-N 0.000 claims 3
- SHGAZHPCJJPHSC-YCNIQYBTSA-N all-trans-retinoic acid Chemical compound OC(=O)\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C SHGAZHPCJJPHSC-YCNIQYBTSA-N 0.000 claims 3
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 claims 3
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 claims 3
- 150000008064 anhydrides Chemical class 0.000 claims 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 3
- 238000006243 chemical reaction Methods 0.000 claims 3
- 230000002255 enzymatic effect Effects 0.000 claims 3
- 239000000284 extract Substances 0.000 claims 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 3
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- QBYIENPQHBMVBV-HFEGYEGKSA-N (2R)-2-hydroxy-2-phenylacetic acid Chemical compound O[C@@H](C(O)=O)c1ccccc1.O[C@@H](C(O)=O)c1ccccc1 QBYIENPQHBMVBV-HFEGYEGKSA-N 0.000 claims 2
- NNRFRJQMBSBXGO-CIUDSAMLSA-N (3s)-3-[[2-[[(2s)-2-amino-5-(diaminomethylideneamino)pentanoyl]amino]acetyl]amino]-4-[[(1s)-1-carboxy-2-hydroxyethyl]amino]-4-oxobutanoic acid Chemical compound NC(N)=NCCC[C@H](N)C(=O)NCC(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(O)=O NNRFRJQMBSBXGO-CIUDSAMLSA-N 0.000 claims 2
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 claims 2
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 claims 2
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- IMQLKJBTEOYOSI-GPIVLXJGSA-N Inositol-hexakisphosphate Chemical compound OP(O)(=O)O[C@H]1[C@H](OP(O)(O)=O)[C@@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@@H]1OP(O)(O)=O IMQLKJBTEOYOSI-GPIVLXJGSA-N 0.000 claims 2
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 claims 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 2
- IMQLKJBTEOYOSI-UHFFFAOYSA-N Phytic acid Natural products OP(O)(=O)OC1C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C1OP(O)(O)=O IMQLKJBTEOYOSI-UHFFFAOYSA-N 0.000 claims 2
- IWYDHOAUDWTVEP-UHFFFAOYSA-N R-2-phenyl-2-hydroxyacetic acid Natural products OC(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-N 0.000 claims 2
- VYGQUTWHTHXGQB-FFHKNEKCSA-N Retinol Palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C VYGQUTWHTHXGQB-FFHKNEKCSA-N 0.000 claims 2
- 239000004480 active ingredient Substances 0.000 claims 2
- 239000013543 active substance Substances 0.000 claims 2
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims 2
- 235000020661 alpha-linolenic acid Nutrition 0.000 claims 2
- 108010089975 arginyl-glycyl-aspartyl-serine Proteins 0.000 claims 2
- 235000010323 ascorbic acid Nutrition 0.000 claims 2
- 239000011668 ascorbic acid Substances 0.000 claims 2
- 229960005070 ascorbic acid Drugs 0.000 claims 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 2
- 239000011575 calcium Substances 0.000 claims 2
- 230000007071 enzymatic hydrolysis Effects 0.000 claims 2
- 238000006047 enzymatic hydrolysis reaction Methods 0.000 claims 2
- 239000004220 glutamic acid Substances 0.000 claims 2
- 235000013922 glutamic acid Nutrition 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- BEJNERDRQOWKJM-UHFFFAOYSA-N kojic acid Chemical compound OCC1=CC(=O)C(O)=CO1 BEJNERDRQOWKJM-UHFFFAOYSA-N 0.000 claims 2
- 229960004705 kojic acid Drugs 0.000 claims 2
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- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims 2
- 229960004488 linolenic acid Drugs 0.000 claims 2
- PRAUVHZJPXOEIF-AOLYGAPISA-N madecassic acid Chemical compound C1[C@@H](O)[C@H](O)[C@@](C)(CO)[C@@H]2[C@H](O)C[C@@]3(C)[C@]4(C)CC[C@@]5(C(O)=O)CC[C@@H](C)[C@H](C)[C@H]5C4=CC[C@@H]3[C@]21C PRAUVHZJPXOEIF-AOLYGAPISA-N 0.000 claims 2
- BUWCHLVSSFQLPN-UHFFFAOYSA-N madecassic acid Natural products CC1CCC2(CCC3(C)C(=CCC4C5(C)CC(O)C(O)C(C)(C5CCC34C)C(=O)O)C2C1C)C(=O)OC6OC(COC7OC(CO)C(OC8OC(C)C(O)C(O)C8O)C(O)C7O)C(O)C(O)C6O BUWCHLVSSFQLPN-UHFFFAOYSA-N 0.000 claims 2
- 229940011656 madecassic acid Drugs 0.000 claims 2
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- 235000011090 malic acid Nutrition 0.000 claims 2
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- 235000002949 phytic acid Nutrition 0.000 claims 2
- 239000000467 phytic acid Substances 0.000 claims 2
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- 108090000765 processed proteins & peptides Proteins 0.000 claims 2
- 102000004196 processed proteins & peptides Human genes 0.000 claims 2
- 229960003471 retinol Drugs 0.000 claims 2
- 235000020944 retinol Nutrition 0.000 claims 2
- 239000011607 retinol Substances 0.000 claims 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims 2
- 235000013311 vegetables Nutrition 0.000 claims 2
- CRDAMVZIKSXKFV-FBXUGWQNSA-N (2-cis,6-cis)-farnesol Chemical compound CC(C)=CCC\C(C)=C/CC\C(C)=C/CO CRDAMVZIKSXKFV-FBXUGWQNSA-N 0.000 claims 1
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- BHQCQFFYRZLCQQ-UHFFFAOYSA-N (3alpha,5alpha,7alpha,12alpha)-3,7,12-trihydroxy-cholan-24-oic acid Natural products OC1CC2CC(O)CCC2(C)C2C1C1CCC(C(CCC(O)=O)C)C1(C)C(O)C2 BHQCQFFYRZLCQQ-UHFFFAOYSA-N 0.000 claims 1
- HJOWVYBCMAYCGY-NAKRPEOUSA-N (4s)-5-[[(2s)-3-carboxy-1-[[(2s)-1-(carboxymethylamino)-3-hydroxy-1-oxopropan-2-yl]amino]-1-oxopropan-2-yl]amino]-5-oxo-4-[[(2s)-5-oxopyrrolidine-2-carbonyl]amino]pentanoic acid Chemical compound OC(=O)CNC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H]1CCC(=O)N1 HJOWVYBCMAYCGY-NAKRPEOUSA-N 0.000 claims 1
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- 229960001153 serine Drugs 0.000 claims 1
- 239000008159 sesame oil Substances 0.000 claims 1
- 235000011803 sesame oil Nutrition 0.000 claims 1
- 239000001540 sodium lactate Substances 0.000 claims 1
- 229940005581 sodium lactate Drugs 0.000 claims 1
- 235000011088 sodium lactate Nutrition 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- 229930003799 tocopherol Natural products 0.000 claims 1
- 239000011732 tocopherol Substances 0.000 claims 1
- 229940042585 tocopherol acetate Drugs 0.000 claims 1
- 235000019149 tocopherols Nutrition 0.000 claims 1
- CRDAMVZIKSXKFV-UHFFFAOYSA-N trans-Farnesol Natural products CC(C)=CCCC(C)=CCCC(C)=CCO CRDAMVZIKSXKFV-UHFFFAOYSA-N 0.000 claims 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 claims 1
- QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 claims 1
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Abstract
본 발명은 하기 일반식(I)의 활성 인지질, 그의 제조 방법. 그를 함유하는 여드름, 건조한 피부, 손상된 피부, 주름진 피부의 손질 및 치료용의 화장품 또는 외피용 조성물에 관한 것이다.
여기서, R1은 특히 포화되거나 또는 1 내지 2개의 불포화기를 갖는 탄소수 14 내지 24개의 지방족쇄를 나타내고, R3는 특히 콜린, 에탈올아민, 글리세롤, 세린, 이노시톨, 에탄올, n-프로판올, n-부탄올 또는 에틸렌글리콜의 잔기를 나타내며, Y는
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (14)
- 하기 일반식 (I)의 활성 인지질.여기서, R1은 특히 포화되거나 또는 1 내지 2개의 불포하기를 갖는 탄소수 14 내지 24개의 지방족쇄를 나타내고, R3는 특히 콜린, 에탈올아민, 글리세롤, 세린, 이노시톨, 에탄올, n-프로판올, n-부탄올 또는 에틸렌글리콜의 잔기를 나타내며, Y는가 포리포리파제의 작용하에 방출된 글리세롤의 2위치에 있는 활성 분자를 나타내는 기이다.
- 제1항에 있어서, R3가 에틸기를 나타내는 것을 특징으로 하는 활성 인지질.
- 제1항에 있어서, 2위치의 활성 분자가 비타민A산, 올-트란스레틴산, 9-시스 레틴산, 13-시스 레틴산, γ-리놀렌산, α-리놀렌산, 에이코사펜탄산(EPA), 도코사헥센산(DHA)등의 필수 지방산, 글루콘산, 만델산, 점액산, 말산, α-페닐락트산, α-히드록시부티르산, 글루콘산, 만델산, 점액산, 말산, α-페닐락트산, 사카린산, 타르트론산 등의 α-히드록시화된 산, 코지산, 아시아산, 마데카쓰산, 벤조산, 글루타민산, 말론산, 피틴산, 아스코르빈산, 노르디히드로과이어레틴산, 살리실산, 18β-글리시레틴산 등의 각종 산, 디로신, 히드록시프롤린, 리신, 아르기닌 등의 아미노산, pyroGlu-Glu-Asp-Ser-GlyOH 또는 Gly-His-Lys 또는 Arg-Gly-Asp-Ser 등의 소시능성 펩타이드 또는 파르네실 숙시네이트, 레티놀 숙시네이트 등의 2가산 모노에스테르 및 일반식 HO2-C-(CH2)n-CO-X-R(여기서, n은 2 내지 16의 수이고, X는 황, 질소 또는 산소 원자를 나타내고 R은 상기 산의 목록에 포함된 기를나타낸다)의 2가산 모노아미드의 분자로 부터 선택됨을 특징으로 하는 활성 인지질.
- 제1항 내지 3항 중 어느 한 항에 있어서, 2위치의 활성 분자가 비타민A산, 리놀렌산, 에이코사펜탄산(EPA), 도코사-헥산산(DHA), 코지산, 아시아산, 마데카쓰산, 글루타민산, 피틴산, 아스코르빈산, 락트산, 글리콜산, 노르디히드로 과이어레틴산, 티로신 등의 아미노산, pyroGlu-Glu-Asp-Ser-GlyOHGly-His-Lys 또는 Arg-Gly-Asp-Ser 등의 소시능성 펩타이드, 18β-글리시레틴산의 물질로 부터 선택되는 것을 특징으로 하는 활성 인지질.
- 천연 공급원으로부터의 하기 일반식(Ⅱ)의 인지질 또는 인지질 혼합물을 효소적 트랜스포스파티딜화 반응시켜 R'3를 에틸, 프로필 또는 부틸기로 치환반응시켜하기 일반식(Ⅲ)의 화합물을 얻고 이 화합물의 글리세롤의 2위치에서 에스테르 기능기를 효소적 가수 분해시켜, 하기 일반식(Ⅳ)의 화합물을 얻고, 얻어진 일반식(Ⅳ)의 화합물의 히드록실기를 하기 일반식 (Ⅴ)의 무수물 또는 대응하는 혼합 무수물로 아실화 반응시키는 것을 특징으로 하는 제1 내지 4항 중 어느 한 항에 따른 일반식(Ⅰ)의 활성 인지질의 제조 방법.여기서, R1및 R2는 동일하거나 상이한 것으로서, 포화되거나 또는 1개 또는 2개의불포화기를 갖는 탄소 원자수 14 내지 24의 지방족쇄를 나타내며, R'3는 콜린, 에탄올아민, 글리세롤, 세린 또는 이노시톨의 잔기를 나타내고, Z는 에틸, 프로필 또는 부틸기를 나타내고,는 제1, 3 및 4항에 정의된 활성 분자의 잔기를 나타낸다.
- 제5항에 있어서, -인지질의 천연 공급원이 난황 또는 식물성 레시틴이고, -천연 공급원으로부터의 인지질이 포스파티딜콜린 또는 포스파티딜에탄올아민 또는이들 인지질의 혼합물이고, -효소적 트랜스포스파티딜화 반응에 의해 수행되는 에틸, 프로필 또는 부틸기에 의한 R'3이 치환이 에탄올, 프로판올 또는 부탄올 매질에서 포스파리파제 D에 의해 이루어지며, 이 반응은 완정하고 단일하며, -일반식(Ⅳ)의 에탄올 리소포스파티딜을 얻기 위한 효소적 가수분해가 Ca++칼슘 매질에서 비정제된 형태로 사용되는 포스파리파제 A2에 의해 수행되며, -일반식(Ⅳ)의 화합물에서 방출된 히드록실기의 세포막으로 이송될 생체 활성 분자(들)에 의한 아실화가에탄올(프로판올 또는 부탄올)리소포스파티딜의 산성화 후에, 예를 들어 디에틸에테르나 톨루엔 등의 용매 중에서 활성 물질의 단순 또는 혼합 무수물을 사용하여 효소적 또는 화학적 경로로 수행됨을 특징으로 하는 활성 인지질의 제조 방법.
- 제5항 또는 6항에 있어서, 2위치에서 인지질에 혼입되는 활성 물질이 제3항에 정의된 물질, 바람직하게는 제4항에 정의된 물질로부터 선택됨을 특징으로 하는 활성 인지질의 제조 방법.
- 제1항 내지 4항 중 어느 한 항에 따른 활성 인지질 및 통상의 부형제를 함유하는 것을 특징으로 하는 피부 특히 여드름으로 고생하는 피부, 건조한 피부, 손상된 피부, 주름진 피부의 손질 및 치료용의 화장품 또는 외피용 조성물.
- 제8항에 있어서, 비타민A산 등의 레티놀 에스테르 또는 그의 이성체를 위한벡타로서 활성 인지질을 함유하는 것을 특징으로 하는 여드름 치료용의 화장품 또는 외피용 조성물.
- 제8항 또는 9항에 있어서, 특히 비타민A팔미테이트, 지용성 선필터의 리놀산, 식물성원의 비누화될 수 없는 물질, 지멘산을 함유하는 유성 혼합물, 참기름의필수 추출물, 과산화 옥수수유, 토코페롤 아세테이트, 천연 토코페롤, 파르네솔로부터 선택된 1종 이상의 보조 지용성 활성 성분을 함유하는 것을 특징으로 하는 화장품 또는 외피용 조성물.
- 제8항 또는 9항에 있어서, 특히 락트산 나트륨, 하프니아 생분해물의 추출물, 클렙셀리아 뉴모니아에 생분해물의 추출물 및 수용성 선 필터로부터 선택된 1종 이상의 보조 수용성 활성 성분을 함유하는 것을 특징으로 하는 화장품 또는 외피용 조성물.
- 제8항 내지 11항 중 어느 한 항에 따른 화장품 또는 외피용 조성물 제조를위한 제1 내지 4항중 어느 한 항에 따른 활성 인지질의 용도.
- 충분한 양의 제8항 내지 11항 중 어느 한 항에 따른 화장품 조성물을 피부에도포하는 것을 특징으로 하는 건조되거나 탈수된 피부의 미용 치료 방법.
- 제9항에 따른 화장품 조성물을 사용함을 특징으로 하는 여드름의 미용 치료방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9315683A FR2714382B1 (fr) | 1993-12-27 | 1993-12-27 | Phospholipides vecteur de molécule active, leur préparation et leur utilisation dans des compositions cosmétiques ou dermatologiques. |
FR93-15683 | 1993-12-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
KR950018021A true KR950018021A (ko) | 1995-07-22 |
Family
ID=9454428
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019940036836A KR950018021A (ko) | 1993-12-27 | 1994-12-26 | 활성 분자를 위한 벡타로서의 인지질. 그의 제조 방법 및 화장품 또는 외피용 조성물에서의 그의 용도 |
Country Status (8)
Country | Link |
---|---|
US (2) | US5985292A (ko) |
EP (1) | EP0659755A1 (ko) |
JP (1) | JPH07206879A (ko) |
KR (1) | KR950018021A (ko) |
AU (1) | AU687931B2 (ko) |
CA (1) | CA2139014A1 (ko) |
FR (1) | FR2714382B1 (ko) |
ZA (1) | ZA9410134B (ko) |
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DE19622224A1 (de) | 1996-02-16 | 1997-08-21 | Max Planck Gesellschaft | Phosphatidyloligoglycerine |
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DE19713793A1 (de) * | 1997-04-03 | 1998-10-08 | Henkel Kgaa | Öl-in-Wasser-Emulsionen zur Wiederherstellung der Lamellarität der Lipidstruktur geschädigter Haut |
FR2777182B1 (fr) * | 1998-04-10 | 2000-06-30 | Lvmh Rech | Compositions cosmetiques ou dermotalogiques pour application topique sous forme d'emulsions de type huile-dans-eau renfermant des esters liquides d'acide gras et d'alcool gras et des phospholipides et leur procede de preparation |
FR2783415B1 (fr) * | 1998-09-18 | 2000-11-03 | Oreal | Composition cosmetique sous forme d'emulsion comprenant une dispersion de particules de polymere stabilisees en surface dans une phase grasse liquide |
FR2785530B1 (fr) * | 1998-11-09 | 2000-12-15 | Oreal | Composition cosmetique sans transfert comprenant une dispersion de particules de polymere et un agent rheologique particulier |
US6395779B1 (en) * | 1999-01-29 | 2002-05-28 | Neoteric Cosmetics, Inc. | Method of treatment using peroxidized lipids |
JP4194196B2 (ja) | 1999-02-22 | 2008-12-10 | 花王株式会社 | 浴用剤組成物 |
US6284802B1 (en) | 1999-04-19 | 2001-09-04 | The Procter & Gamble Company | Methods for regulating the condition of mammalian keratinous tissue |
FR2794466B1 (fr) * | 1999-06-02 | 2001-06-29 | Oreal | Composition sous forme d'emulsion huile-dans-eau contenant des fibrilles de cellulose et ses utilisations notamment cosmetiques |
GB9918023D0 (en) * | 1999-07-30 | 1999-09-29 | Unilever Plc | Skin care composition |
JP4523747B2 (ja) * | 1999-08-24 | 2010-08-11 | 花王株式会社 | 化粧料 |
CA2429817C (en) | 2000-11-24 | 2013-02-12 | Vascular Biogenics Ltd. | Methods employing and compositions containing defined oxidized phospholipids for prevention and treatment of atherosclerosis |
US6838452B2 (en) | 2000-11-24 | 2005-01-04 | Vascular Biogenics Ltd. | Methods employing and compositions containing defined oxidized phospholipids for prevention and treatment of atherosclerosis |
ITMI20011022A1 (it) * | 2001-05-17 | 2002-11-17 | Indena Spa | Composizioni farmaceutiche e cosmetiche contro l'invecchiamento cutaneo |
DE10133202A1 (de) * | 2001-07-07 | 2003-01-16 | Beiersdorf Ag | Osmolyte enthaltende kosmetische und dermatologische Zubereitungen zur Behandlung und aktiven Prävention trockener Haut und anderer negativer Veränderungen der physiologischen Homöostase der gesunden Haut |
ITMI20021280A1 (it) * | 2002-06-11 | 2003-12-11 | Carlo Ghisalberti | Metodo di trattamento anticellulite |
JP4653513B2 (ja) * | 2004-02-25 | 2011-03-16 | 株式会社コーセー | 皮膚外用剤 |
US7807847B2 (en) * | 2004-07-09 | 2010-10-05 | Vascular Biogenics Ltd. | Process for the preparation of oxidized phospholipids |
EP2604614B1 (en) | 2004-07-09 | 2016-03-09 | Vascular Biogenics Ltd. | Oxidized phospholipids |
US7763264B2 (en) * | 2005-04-26 | 2010-07-27 | John Kulesza | Composition and method for reducing the appearance of cellulite |
WO2007079394A2 (en) * | 2005-12-30 | 2007-07-12 | Revance Therapeutics, Inc. | Arginine heteromers for topical administration |
JP4879834B2 (ja) * | 2006-10-12 | 2012-02-22 | 日揮触媒化成株式会社 | 多機能性複合粉体を配合してなる化粧料 |
US8569529B2 (en) | 2007-01-09 | 2013-10-29 | Vascular Biogenics Ltd. | High-purity phospholipids |
US9006217B2 (en) | 2007-01-09 | 2015-04-14 | Vascular Biogenics Ltd. | High-purity phospholipids |
US7321064B1 (en) * | 2007-03-08 | 2008-01-22 | Cedarburg Pharmaceuticals, Inc. | Preparation of amides of retinoic acid via mixed anhydride and mixed carbonate intermediates |
CN102271517B (zh) * | 2008-11-06 | 2015-04-08 | 脉管生物生长有限公司 | 氧化的脂质化合物和其用途 |
GB2486371A (en) * | 2009-08-21 | 2012-06-13 | Targeted Delivery Technologies Ltd | Vesicular formulations |
RS59380B1 (sr) * | 2011-06-08 | 2019-11-29 | Nitto Denko Corp | Jedinjenja za ciljanje isporuke leka i pojačavanje sirnk aktivnosti |
WO2013015288A1 (ja) * | 2011-07-26 | 2013-01-31 | ナガセケムテックス株式会社 | リパーゼ活性阻害剤 |
GB201205642D0 (en) | 2012-03-29 | 2012-05-16 | Sequessome Technology Holdings Ltd | Vesicular formulations |
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US9771385B2 (en) | 2014-11-26 | 2017-09-26 | Vascular Biogenics Ltd. | Oxidized lipids |
ES2855299T3 (es) | 2014-11-26 | 2021-09-23 | Vascular Biogenics Ltd | Lípidos oxidados y tratamiento o prevención de la fibrosis |
EP3954361A1 (en) | 2015-06-30 | 2022-02-16 | Sequessome Technology Holdings Limited | Multiphasic compositions |
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DE36583C (de) * | ZIMMERMANN & BUCH-LOH in Berlin N., Uferstr. 6 | Neuerung an Weichen- und Signal-Sicherungs-Apparaten | ||
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US4882165A (en) * | 1981-11-09 | 1989-11-21 | The Regents Of The University Of California | Light sensitive liposomes |
FR2517310A1 (fr) * | 1981-11-27 | 1983-06-03 | Unilever Nv | Derives d'a-glycerophosphatidester, procede pour leur preparation, composition cosmetique ou pharmaceutique les contenant |
US4471113A (en) * | 1982-02-03 | 1984-09-11 | The United States Of America As Represented By The Department Of Energy | Prodrugs based on phospholipid-nucleoside conjugates |
DE3346525C2 (de) * | 1983-12-22 | 1987-03-19 | A. Nattermann & Cie GmbH, 5000 Köln | Pharmazeutische Zubereitung mit speziellen 1,2-Diacyl-glycero-3-phosphocholinen zur Behandlung von Erkrankungen im Magen-Darmbereich |
FR2563431B1 (fr) * | 1984-04-26 | 1987-03-06 | Roussel Uclaf | Nouvelles compositions cosmetiques renfermant des extraits lyses d'hafnia |
EP0237051B1 (en) * | 1986-03-14 | 1991-05-02 | Fujisawa Pharmaceutical Co., Ltd. | Prodrug compounds, process for the preparation thereof and sustained release preparation comprising the same |
IT1203515B (it) * | 1987-02-26 | 1989-02-15 | Indena Spa | Complessi di saponine con fosfolipidi e composizioni farmaceutiche e cosmetiche che li contengono |
US5093360A (en) * | 1989-04-07 | 1992-03-03 | Yu Ruey J | Retinal, derivatives and their therapeutic use |
US5075340A (en) * | 1989-05-22 | 1991-12-24 | Iowa State University Research Foundation | Retinoic acid glucuronide preparations for application to the skin |
US5194654A (en) * | 1989-11-22 | 1993-03-16 | Vical, Inc. | Lipid derivatives of phosphonoacids for liposomal incorporation and method of use |
US5411947A (en) * | 1989-06-28 | 1995-05-02 | Vestar, Inc. | Method of converting a drug to an orally available form by covalently bonding a lipid to the drug |
JPH03153628A (ja) * | 1989-11-13 | 1991-07-01 | Nippon Oil & Fats Co Ltd | 高度不飽和脂肪酸含有脂質の可溶化組成物 |
AU7872491A (en) * | 1990-05-07 | 1991-11-27 | Vical, Inc. | Lipid prodrugs of salicylate and nonsteroidal anti-inflammatory drugs |
US5643600A (en) * | 1991-09-17 | 1997-07-01 | Micro-Pak, Inc. | Lipid vesicles containing avocado oil unsaponifiables |
JP3087271B2 (ja) * | 1995-07-31 | 2000-09-11 | 日本精機株式会社 | Fpc板接続装置 |
-
1993
- 1993-12-27 FR FR9315683A patent/FR2714382B1/fr not_active Expired - Fee Related
-
1994
- 1994-12-20 ZA ZA9410134A patent/ZA9410134B/xx unknown
- 1994-12-21 EP EP94402975A patent/EP0659755A1/fr not_active Withdrawn
- 1994-12-22 AU AU81709/94A patent/AU687931B2/en not_active Ceased
- 1994-12-23 CA CA002139014A patent/CA2139014A1/fr not_active Abandoned
- 1994-12-26 KR KR1019940036836A patent/KR950018021A/ko active IP Right Grant
- 1994-12-27 JP JP6336868A patent/JPH07206879A/ja active Pending
-
1996
- 1996-12-24 US US08/773,720 patent/US5985292A/en not_active Expired - Lifetime
-
1999
- 1999-08-18 US US09/376,323 patent/US6133463A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH07206879A (ja) | 1995-08-08 |
FR2714382A1 (fr) | 1995-06-30 |
EP0659755A1 (fr) | 1995-06-28 |
AU8170994A (en) | 1995-07-06 |
AU687931B2 (en) | 1998-03-05 |
CA2139014A1 (fr) | 1995-06-28 |
FR2714382B1 (fr) | 1996-02-02 |
ZA9410134B (en) | 1995-12-20 |
US6133463A (en) | 2000-10-17 |
US5985292A (en) | 1999-11-16 |
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